Regulatory affairs courses, webinars, conferences and meetings

We offer a comprehensive programme of training courses, conferences, meetings and webinars on a wide range of regulatory affairs topics.

Our courses are delivered by highly regarded experts from industry and government agencies and are suitable for professionals at all stages of their regulatory career. Read more about the different regulatory affairs course categories and how these relate to your own career.

Our commitment to quality

TOPRA is proud to have provided gold standard training for regulatory affairs professionals for more than 40 years. Our commitment to the profession, to everyone who attends our training and to employers who entrust their staff development to us, is given in our Quality Statement.

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27/10/2021Biotech SPIN Webinar: Risk Based Approach To ATMPsFollowing on from the successful webinar on the Clinical Development on ATMPs on 7 April, Dr Bridget Heelan returns with a follow up presentation. OnlineBIOOCT21
27/10/2021Sponsored: An integrated approach to regulatory submissionsFREE SPONSORED WEBINAR - The success of regulatory submissions is dependent on the close collaboration between regulatory, supply, and quality teams. Breaking down silos, and working together to plan and execute effective marketing authorization supply transfers (MAST) enables a seamless supply of compliant drugs and devices to reach patients around the world. OnlineSPOWEBGP
27/10/2021Sponsored: An integrated approach to regulatory submissionsFREE SPONSORED WEBINAR - The success of regulatory submissions is dependent on the close collaboration between regulatory, supply, and quality teams. Breaking down silos, and working together to plan and execute effective marketing authorization supply transfers (MAST) enables a seamless supply of compliant drugs and devices to reach patients around the world. OnlineSPOWEBHVIV
28/10/2021Essentials of European Pharmaceutical Regulatory AffairsThis course will provide a basic but comprehensive overview of pharmaceutical regulatory affairs in a relaxed and interactive environment.LondonUnited KingdomBAS2810
28/10/2021Essentials of European Pharmaceutical Regulatory AffairsThis course will provide a basic but comprehensive overview of pharmaceutical regulatory affairs in a relaxed and interactive environment. OnlineVBAS1021
28/10/2021TOPRA In Scotland - Clinical TrialsThis TOPRA in Scotland meeting will be held via webinar, and will include presentations on the supply of comparators and other licensed medicines for clinical trials, and the pros and cons of blinding in clinical trials, with time for a Q&A session. OnlineSCOOCT21
29/10/2021Regulatory Framework for COVID vaccine development in IndiaTOPRA in INDIA steering group invites to you to join this Member Webinar focussing on the Regulatory framework for COVID vaccine development in India with guest speaker, Varma Bhupathiraju. OnlineTI10
02/11/2021The Autumn Introductory Course (Pharmaceuticals)Module 0 of the MSc: This course covers all aspects of the product development process, and provides a sound overview of EU legislation and regulatory procedures, including the central role regulatory affairs plays in modern healthcare companies. OnlineVIC22021
09/11/2021Essentials of European Medical Device Regulatory AffairsThis course will provide an overview of regulatory requirements and considerations for medical devices in a relaxed and interactive environment. OnlineVMDBASRE21
10/11/2021Webinar: Regulatory Requirements of JapanThis webinar will provide the attendee with a high-level operational understanding of the medicine and related products regulatory landscape in Japan. OnlineWEBMEDJP
11/11/2021Sponsored: The Changing Landscape of Regulatory AffairsFREE SPONSORED WEBINAR -  Navigating the ever changing landscape of Regulatory Affairs, Roche this webinar will include: Applying Project Orbis, Electronic Product Labelling, the new Clinical Trial Regulation and how Medical Writing is evolving. OnlineSPOWEBROCH
12/11/2021Sponsored: Manufacturing & Regulatory challenges in ATMPsFREE SPONSORED WEBINAR -  Pharmalex highlight the challenges encountered during the manufacturing of Cell, tissue and gene therapy (CGT) medicinal products / Advanced Therapy Medicinal Products (ATMPs) and the key regulatory support required to facilitate bringing these therapies to the market. OnlineSPOWEBPLX
16/11/2021Sponsored: The worlds first Covid-19 Human Challenge TrialFREE SPONSORED WEBINAR -  The worlds first Covid-19 Human Challenge Trial: The Regulatory challenges. This webinar will navigate through the regulatory strategy that resulted in the approval and execution the world’s first Covid-19 human challenge trial, in which healthy volunteers where deliberately infected with SARS-CoV-2. You will be taken step-by-step through the regulatory approach, from the manufacturing of the human challenge agent, over the Scientific Advice meetings with Regulators, to the Clinical Trial Approval and the discussions with the Ethics Committee. OnlineSPOWEBHV
16/11/2021TOPRA In Sweden - Medical Devices: New Regulations for IVDRThis evening is an ideal opportunity to discuss the new In Vitro Diagnostic Medical Devices Regulation (IVDR), which will be fully implemented from 26 May 2022. Background and EU Commission perspective. How is the work at the Medical Products Agency affected and how do the companies prepare? What applies to clinical performance studies on IVD products? OnlineSWENOV21
17/11/2021TOPRA In CEE-Herbal Medicinal Products Regulatory LandscapePlease join Alenka Drazumeric from our TOPRA In Central Eastern Europe network who will present this informative webinar covering an  'Overview of Herbal Medicinal Products Regulatory Landscape in Europe'. OnlineCEE21
18/11/2021The TOPRA Awards for Excellence 2021 - Nominee RegistrationCongratulations on being a Finalist! Join us at The Royal Institute of British Architects (RIBA) on 18 November for the Awards for Regulatory Excellence to celebrate the achievements of individuals, teams and organisations in the regulatory affairs community.London AWARDNOM21
18/11/2021The Awards for Regulatory ExcellenceJoin us at the Royal Institute of British Architects (RIBA) on 18 November for the Awards for Regulatory Excellence to celebrate the achievements of individuals, teams and organisations in the regulatory affairs community.LondonUnited KingdomAWARDS21
19/11/2021TOPRA In India - Roles and Limitation of AIThis TOPRA In India webinar will explore the roles and limitations of Artificial Intelligence in Regulatory Intelligence in this informative session with guest speaker Dharmesh Kharwar– Founder and Director at NGB Laboratories Ltd. OnlineTII11
26/11/2021CPD and Professional RegistrationA skills based workshop designed for apprentices following the Regulatory Affairs Specialist training programme. OnlineCPD21
30/11/2021Medical Device Regulatory Requirements in CanadaThe webinar will provide a high-level overview of the regulatory environment for medical devices in Canada, including regulatory authorization pathways and post-market requirements. OnlineWEBMDCND
01/12/2021Data Management and Digitalisation in Regulatory AffairsModule 12 of the MSc and Masterclass: This Masterclass will provide you with  the theoretical background to data management, document management, electronic submissions, eCompliance regulatory information management and the new identification of Medicinal Products (IDMP) requirements, and find solutions to practical problems in this area. Deal with large volumes of data and deal with different data (from nonclinical to post-market pharmacovigilance).LondonUnited KingdomMSCM1221NE
01/12/2021Data Management and Digitalisation in Regulatory AffairsModule 12 of the MSc and Masterclass: This Masterclass will provide you with  the theoretical background to data management, document management, electronic submissions, eCompliance regulatory information management and the new identification of Medicinal Products (IDMP) requirements, and find solutions to practical problems in this area. Deal with large volumes of data and deal with different data (from nonclinical to post-market pharmacovigilance). OnlineMSCM1221O
02/02/2022Regulatory Requirements for a New Active Substance: QualityThis Masterclass is also Module 3 of the TOPRA MSc Regulatory Affairs and will help you understand and provide advice on quality data requirements in the pharmaceutical regulatory environment as well as address practical regulatory questions in this area.CheshamUnited KingdomMSC32022
02/02/2022Regulatory Requirements for a New Active Substance: QualityThis Masterclass is also Module 3 of the TOPRA MSc Regulatory Affairs and will help you understand and provide advice on quality data requirements in the pharmaceutical regulatory environment as well as address practical regulatory questions in this area. OnlineMSCM32022O
08/02/2022Essentials of European Veterinary Regulatory AffairsThe world of veterinary regulatory affairs can be a confusing and complex place, particularly if you have no formal veterinary or regulatory affairs background. The purpose of this course is to provide you with a clear and concise understanding of the role played by regulatory affairs in obtaining and maintaining marketing authorisation for veterinary medicinal products.LondonUnited KingdomVETBAS22
08/02/2022Essentials of European Veterinary Regulatory AffairsThe world of veterinary regulatory affairs can be a confusing and complex place, particularly if you have no formal veterinary or regulatory affairs background. The purpose of this course is to provide you with a clear and concise understanding of the role played by regulatory affairs in obtaining and maintaining marketing authorisation for veterinary medicinal products. OnlineVETBAS22O
15/02/2022CRED Regulatory Document Writing and ManagementSkills based course on the theory and practice of writing regulatory documents and communications for optimal impact and effectiveness.LondonUnited KingdomDOC22
15/02/2022CRED Regulatory Document Writing and ManagementSkills based course on the theory and practice of writing regulatory documents and communications for optimal impact and effectiveness. OnlineDOC22O
23/02/2022CRED European IVD Regulatory AffairsThis two and a half day interactive course will cover all the key topics and areas of responsibility for professionals taking on the Person Responsible for Regulatory Compliance role under the IVDR. It will also provide comprehensive information for anyone responsible for implementing the necessary changes to be ready when the IVDR comes into force.LondonUnited KingdomIVD222
23/02/2022CRED European IVD Regulatory AffairsThis two and a half day interactive course will cover all the key topics and areas of responsibility for professionals taking on the Person Responsible for Regulatory Compliance role under the IVDR. It will also provide comprehensive information for anyone responsible for implementing the necessary changes to be ready when the IVDR comes into force. OnlineIVD222O